BEUDAMED
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    DYNESYS TOP LOADING

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code LXH·February 6, 2009

    CANNULATED POLYAXIAL SCREW 6.5MM X 35MM

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code NKB·April 7, 2014

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    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC·Product code MAX·May 1, 2014

    ARDIS PEEK IMPLANT 08X09X22

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code MAX·June 20, 2014

    3.5MM X 24MM PRIMARY OPEN POLY SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code NKB·April 11, 2014

    TRINICA SCREW SELF-DRILLING VARIABLE 4.2X14

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code KWQ·May 14, 2014

    SPECIALTY HEX DRIVER, RING RETAINER

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HXX·March 3, 2010

    TITLE2

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HXX·April 23, 2010

    SEQUOIA SCREWDRIVER, MODULAR

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HXX·May 27, 2010

    ARDIS INSERTER - 9MM

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code MAX·June 17, 2014

    ARDIS PEEK IMPLANT 12X09X26

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code MAX·December 18, 2014

    SEQUOIA TI POLY SCREW ASSY 6.5 MM X 45 MM

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code NKB·November 14, 2014

    TRINICA DRILL BIT, 2.3, STERILE, ATO

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HTW·May 2, 2012

    ARDIS INSERTER - 9MM

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code MAX·December 18, 2014

    ARDIS GENERIC

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code KWP·October 2, 2014

    ST360 SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code KWQ·April 10, 2007

    TRINICA ATO INSTRUMENT

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HXY·April 5, 2007

    TRINICA CERVICAL BONE TAP

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HWX·November 20, 2009

    TITLE II LOCKING SCREW DRIVER

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code HXX·October 22, 2009

    ST360

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC.·Product code KWQ·October 16, 2009